Viability and enzymatic activity of cryopreserved porcine heart valve.
10.3349/ymj.1999.40.2.184
- Author:
Hwal SUH
1
;
Jong Eun LEE
;
Jong Chul PARK
;
Dong Wook HAN
;
Chee Soon YOON
;
Young Hwan PARK
;
Bum Koo CHO
Author Information
1. Department of Medical Engineering, Yonsei University College of Medicine, Seoul, Korea. hwal@yumc.yonsei.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Porcine valve;
viability;
enzymatic activity;
tissue preservation;
cryopreservation
- MeSH:
Animal;
Cryopreservation*;
Heart Valves/physiology*;
Heart Valves/enzymology*;
Swine;
Tissue Survival/physiology*
- From:Yonsei Medical Journal
1999;40(2):184-190
- CountryRepublic of Korea
- Language:English
-
Abstract:
Fibroblast viability of a natural tissue valve for replacing a defective heart valve through allograft or xenograft has been suggested to affect its clinical durability. In this study, the cell viability and enzymatic activity of porcine heart valve leaflets were examined in regard to concerning to the preservation process [variable warm ischemic time (WIT), cold ischemic time (CIT), and cryopreservation]. Porcine heart enblocs were obtained and valve dissection was performed after 2, 12, 24, or 36 hours, in respective groups A, B, C, and D, as WIT. Each group was stored for 24 hours as CIT and cryopreserved. Leaflets were dissected from a valved conduit after each process, and cell viability and enzymatic activity in the leaflet were investigated using trypan blue staining and API ZYM kits. WIT extension significantly decreased fibroblast viability (p < 0.05, 92.25 +/- 2.7% at 2 hours, 84.9 +/- 6.7% at 12 hours, 57.0 +/- 10.2% at 24 hours, 55.9 +/- 7.9% at 36 hours), while CIT for 24 hours was also influenced significantly (p < 0.05), whereas cryopreservation demonstrated no effect on cellular viability. In enzyme activity observation, several enzymes related to lipid or nucleotide degradation (esterase, esterase lipase, particularly phosphatase, phosphohydrolase) were remarkably changed following the valve-fabrication process. After 24 hours CIT, these enzymatic activities in groups B, C and D significantly increased, but the activities decreased after cryopreservation. Particularly, both the viability and enzymatic activity showed remarkable changes after CIT in group B (WIT = 12 hours). These results suggest that WIT is more important than CIT in maintaining viability of the valve, and that completing all the cryopreservation process within 12 hours after acquisition is recommended.
